WILSON'S DISEASE: A GENETIC DISORDER OF COPPER METABOLISM

Wilson's Disease: A Genetic Disorder of Copper Metabolism

Wilson disorder, a genetic illness affecting copper regulation, presents a complex set of manifestations. This infrequent condition causes the build-up of copper in various parts of the body, primarily the liver, brain, and vision. People with Wilson disease may display a wide range of symptoms, including liver damage, brain impairments, and visual

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Wilson Disease: A Genetic Disorder of Copper Metabolism

Wilson disorder, a hereditary illness affecting copper processing, presents a unique set of signs. This infrequent condition causes the build-up of copper in various tissues of the body, primarily the liver, brain, and eyes. People with Wilson disease may experience a varied range of symptoms, including hepatic failure, neurological impairments, an

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